Benzyl gentiobioside: Difference between revisions
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'''Benzyl gentiobioside''' is a decyanogenated form of [[amygdalin]].<ref name =dc>{{cite journal |last1=Del Cueto |first1=Jorge |last2=Ionescu |first2=Irina A. |last3=Pičmanová |first3=Martina |last4=Gericke |first4=Oliver |last5=Motawia |first5=Mohammed S. |last6=Olsen |first6=Carl E. |last7=Campoy |first7=José A. |last8=Dicenta |first8=Federico |last9=Møller |first9=Birger L. |last10=Sánchez-Pérez |first10=Raquel |title=Cyanogenic Glucosides and Derivatives in Almond and Sweet Cherry Flower Buds from Dormancy to Flowering |journal=Frontiers in Plant Science |date=19 May 2017 |volume=8 |pages=800 |doi=10.3389/fpls.2017.00800|url = https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5437698/}}</ref> Benzyl gentiobioside occurs in ''[[Prunus persica]]'' seeds.<ref name =dc/> |
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'''Benzyl Gentiobioside''' is a decyanogenated form of [[Amygdalin]] |
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==References== |
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{{Reflist}} |
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Revision as of 05:30, 16 May 2021
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IUPAC name
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-phenylmethoxyoxan-2-yl]methoxy]oxane-3,4,5-triol
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Identifiers | |
3D model (JSmol)
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ChemSpider | |
PubChem CID
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CompTox Dashboard (EPA)
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Properties | |
C19H28O11 | |
Molar mass | 432.422 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Benzyl gentiobioside is a decyanogenated form of amygdalin.[1] Benzyl gentiobioside occurs in Prunus persica seeds.[1]
References
- ^ a b Del Cueto, Jorge; Ionescu, Irina A.; Pičmanová, Martina; Gericke, Oliver; Motawia, Mohammed S.; Olsen, Carl E.; Campoy, José A.; Dicenta, Federico; Møller, Birger L.; Sánchez-Pérez, Raquel (19 May 2017). "Cyanogenic Glucosides and Derivatives in Almond and Sweet Cherry Flower Buds from Dormancy to Flowering". Frontiers in Plant Science. 8: 800. doi:10.3389/fpls.2017.00800.
{{cite journal}}
: CS1 maint: unflagged free DOI (link)